Canonical Allele Identifier: PA658681480
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 479921
ClinVar RCV Id: RCV000572899 RCV000797361
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Lys1296Gln
CA072260
NM_000179.3:c.3886A>C